2-Amino-4,6-dichloropyrimidine → 4-Chloro-6-(2-furanyl)-2-pyrimidinamine
반응식
C([Sn](CCCC)(CCCC)[C:6]1[O:7][CH:8]=[CH:9][CH:10]=1)CCC.[NH2:19][C:20]1[N:25]=[C:24](Cl)[CH:23]=[C:22]([Cl:27])[N:21]=1>CN(C=O)C.Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1>[NH2:19][C:20]1[N:21]=[C:22]([Cl:27])[CH:23]=[C:24]([C:6]2[O:7][CH:8]=[CH:9][CH:10]=2)[N:25]=1참가 물질
반응 조건
- 온도
- 80 °C
실험 절차
A solution of 2-(tributylstannyl)furan (35.7 g, 100 mmol) in DMF (100 mL) was treated with 2-amino-4,6-dichloropyrimidine (16.4 g, 100 mmol) and dichlorobis(triphenylphosphine)palladium (II) (3.51 g, 5.0 mmol). The suspension was stirred at 80° C. for 18 h, allowed to cool to room temperature and poured onto ice (400 g). The solid precipitate was filtered off, washed with water, dried in air, and the filtrate was extracted with EtOAc (300 mL), washed with water (100 mL), mixed with the solid precipitate and concentrated. The crude product was purified by chromatography [SiO2; EtOAc:toluene (0:1-1:9-2:3)] and the material with Rf 0.23 (isopropyl ether) was triturated with isohexane to give the title compound (11.1 g, 57%) as a yellow solid; mp. 133-140° C.; NMR δH (400 MHz, DMSO) 6.70 (1H, q, J 2.0 Hz), 6.95 (1H, s), 7.16 (2H, br s), 7.27 (1H, d, J 3.6 Hz) and 7.92 (1H, t, J 1.0 Hz).
후처리
- temperatureto cool to room temperature
- additionpoured onto ice (400 g)
- filtrationThe solid precipitate was filtered off
- washwashed with water
- customdried in air
- extractionthe filtrate was extracted with EtOAc (300 mL)
- washwashed with water (100 mL)
- additionmixed with the solid precipitate
- concentrationconcentrated
- customThe crude product was purified by chromatography [SiO2; EtOAc:toluene (0:1-1:9-2:3)]
- customthe material with Rf 0.23 (isopropyl ether) was triturated with isohexane
출처 및 근거
- ORD 기록
- ord-b47238b752264867847b322086626272
- 출처 데이터셋
- uspto-grants-2011_01
- 특허 번호
- US07875600B2
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